On the public citation graph
A new system for the designation of chemical compounds. 1. Theoretical preliminaries and the coding of acyclic compounds
0 signed · 36 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/bkcs.10334openalex-snapshot
Universal Structure Conversion Method for Organic Molecules: From Atomic Connectivity to Three‐Dimensional Geometry
inferred← citeshttps://doi.org/10.1002/jcc.23300openalex-snapshot
Common vertex matrix: A novel characterization of molecular graphs by counting
inferred← citeshttps://doi.org/10.1002/jcc.23413openalex-snapshot
On the centrality of vertices of molecular graphs
inferred← citeshttps://doi.org/10.1002/qua.560300718openalex-snapshot
On the identification numbers for chemical structures
inferred← citeshttps://doi.org/10.1002/qua.560300762openalex-snapshot
On some solved and unsolved problems of chemical graph theory
inferred← citeshttps://doi.org/10.1007/0-306-46907-3_6openalex-snapshot
On Characterization of 3D Molecular Structure
inferred← citeshttps://doi.org/10.1007/bf01164196openalex-snapshot
Computer generation of acyclic graphs based on local vertex invariants and topological indices. Derived canonical labelling and coding of trees and alkanes
inferred← citeshttps://doi.org/10.1007/bf01164472openalex-snapshot
Central vertices versus central rings in polycyclic systems
inferred← citeshttps://doi.org/10.1007/bf01164840openalex-snapshot
In search of structural invariants
inferred← citeshttps://doi.org/10.1007/bf01166045openalex-snapshot
A review and examination of the mathematical spaces underlying molecular similarity analysis
inferred← citeshttps://doi.org/10.1007/bf01166925openalex-snapshot
On the recognition of structural features: Some general problems illustrated by hamiltonian paths in polyhexes
inferred← citeshttps://doi.org/10.1007/s10288-002-0008-9openalex-snapshot
Chemical trees enumeration algorithms
inferred← citeshttps://doi.org/10.1007/s10910-013-0255-3openalex-snapshot
Canonical labels for protein spots of proteomics maps
inferred← citeshttps://doi.org/10.1016/0003-2670(95)00359-2openalex-snapshot
A new topological index for the Changchun Institute of Applied Chemistry 13C NMR information system
inferred← citeshttps://doi.org/10.1016/0022-2860(93)87047-dopenalex-snapshot
In search for graph invariants of chemical interes
inferred← citeshttps://doi.org/10.1016/0097-8485(94)85010-0openalex-snapshot
Coding of chemical structures based on a line notation
inferred← citeshttps://doi.org/10.1016/0166-1280(88)87021-0openalex-snapshot
Compact molecular codes for polycyclic systems
inferred← citeshttps://doi.org/10.1016/0166-1280(89)85005-5openalex-snapshot
Do chemical graphs have a natural order? some regularities of a “compacted maximal adjacency code”
inferred← citeshttps://doi.org/10.1016/0166-1280(89)85011-0openalex-snapshot
The concept for the centre of a chemical structure and its applications
inferred← citeshttps://doi.org/10.1016/0166-1280(93)80012-oopenalex-snapshot
Topological/chemical distances and graph centers in molecular graphs with multiple bonds
inferred← citeshttps://doi.org/10.1016/0166-1280(95)04139-7openalex-snapshot
The boundary-edges code for polyhexes
inferred← citeshttps://doi.org/10.1016/0166-218x(88)90004-2openalex-snapshot
Determining structural similarity of chemicals using graph-theoretic indices
inferred← citeshttps://doi.org/10.1016/0166-218x(95)00022-jopenalex-snapshot
Chemistry and discrete mathematics
inferred← citeshttps://doi.org/10.1016/0898-5529(90)90105-hopenalex-snapshot
A language for acyclic groups
inferred← citeshttps://doi.org/10.1016/j.ympev.2009.04.019openalex-snapshot
BOOL-AN: A method for comparative sequence analysis and phylogenetic reconstruction
inferred← citeshttps://doi.org/10.1016/s0009-2614(97)00447-8openalex-snapshot
Characterization of 3-D sequences of proteins
inferred← citeshttps://doi.org/10.1021/ci00025a001openalex-snapshot
Chemical Graphs: Looking Back and Glimpsing Ahead
inferred← citeshttps://doi.org/10.1021/ci00047a023openalex-snapshot
Historic development of chemical notations
inferred← citeshttps://doi.org/10.1021/ci990422wopenalex-snapshot
SMILES Extensions for Pattern Matching and Molecular Transformations: Applications in Chemoinformatics
inferred← citeshttps://doi.org/10.1023/a:1019143307939openalex-snapshot
On structural ordering and branching of acyclic saturated hydrocarbons
inferred← citeshttps://doi.org/10.1142/s1793830924500782openalex-snapshot
A new spectral-based index for graphs and its application to polyaromatic compounds
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.